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In addition, the random copolyester analogs of the hard block are examined. The ester segments are composed of two isomers, poly(tetramethylene terephthalate) (PTMT) and poly(tetramethylene isophthalate) (PTMI), which possess significantly different crystallization kinetics. The ratio of PTMT to PTMI in the series has been systematically varied to alter the crystallizability without changing the chemical composition. The results of differential scanning calorimetry, wide‐angle x‐ray diffraction, and dynamic mechanical characterization are presented. Copolymerization of a second ester shortens the average sequence length of the first ester, resulting in melting‐point depression for crystals of the first polyester and substantial lowering of the dynamic mechanical storage modulus above the glass transition of the intercrystalline phase. The melting‐point depression may be predicted by using Flory's model for random copolymers, but the calculated heats of fusion are significantly lower than those obtained from diluent melting‐point depression.\u003C\u002Fjats:p>",{"EN":43},"Thermal and mechanical properties of short‐segment block copolyesters and copolyether–esters",{"VOID":45},"10.1002\u002Fpol.1985.180231010",{"VOID":47},"[\"9013290251621082107\"]","PUBLICATION","VERIFIED","Auto Verify",[52],"EN","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fpol.1985.180231010",[55,79,94,110],{"id":56,"sortIndex":57,"researcher":19,"roles":58,"affiliations":59,"properties":72},"a579de89-f118-4e22-9c51-4b204eec8e4b",3,[],[60],{"id":61,"sortIndex":20,"affiliation":62,"properties":19},"fc44cccb-4058-4694-adc9-2374198cf4bd",{"id":63,"createTime":64,"updateTime":65,"relativeEntities":66,"slug":67,"properties":68,"entityType":71,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"5065ee45-4caa-4a43-8d32-f1d5bd91caec","2023-12-29T11:41:00.966+00:00","2024-10-16T16:25:34.253+00:00",[],"Department-of-Chemical-Engineering-University-of-Wisconsin-Madison-Wisconsin-53706",{"title":69},{"VI":70},"Department of Chemical Engineering, University of Wisconsin, Madison, Wisconsin 53706","AFFILIATION",{"openalex":73,"orcid":75,"title":77},{"VOID":74},"A5021289418",{"VOID":76},"https:\u002F\u002Forcid.org\u002F0000-0003-4316-3347",{"EN":78},"Stuart L. 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K., Rubber Chem. Technol.",{},{"id":19,"text":159,"url":19,"identifiers":160},"C.Tanaka M.Hiratsuka H.Kobayashi andM.Kitanaka to appear.",{},{"id":19,"text":162,"url":19,"identifiers":163},"10.1002\u002Fapp.1980.070250513",{"doi":162},{"id":19,"text":165,"url":19,"identifiers":166},"Buck W. H., 1973, Polym. Prepr. Am. Chem. Soc. Div. Polym. 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Elastomer Chemicals Department Contribution No. 311.",{},{"id":19,"text":198,"url":19,"identifiers":199},"10.1016\u002F0032-3861(78)90063-0",{"doi":198},{"id":19,"text":201,"url":19,"identifiers":202},"10.1002\u002Fpol.1959.1204013720",{"doi":201},{"id":19,"text":204,"url":19,"identifiers":205},"Alexander L., 1969, X‐Ray Diffraction Methods in Polymer Science",{},{"id":19,"text":207,"url":19,"identifiers":208},"Kakudo M., 1972, X‐Ray Diffraction by Polymers",{},{"id":19,"text":210,"url":19,"identifiers":211},"Lonsdale K., 1962, International Tables for X‐Ray Crystallography",{},{"id":19,"text":213,"url":19,"identifiers":214},"10.1016\u002F0032-3861(84)90245-3",{"doi":213},{"id":19,"text":216,"url":19,"identifiers":217},"10.1002\u002Fpol.1976.180141117",{"doi":216},{"id":19,"text":219,"url":19,"identifiers":220},"10.1016\u002F0032-3861(77)90189-6",{"doi":219},{"id":19,"text":222,"url":19,"identifiers":223},"10.1063\u002F1.1747230",{"doi":222},{"id":19,"text":225,"url":19,"identifiers":226},"McCrum N. G., 1967, Anelastic and Dielectric Effects in Polymeric Solids",{},{"id":19,"text":228,"url":19,"identifiers":229},"10.1002\u002Fapp.1976.070200507",{"doi":228},{"id":19,"text":231,"url":19,"identifiers":232},"10.1016\u002F0095-8522(63)90100-4",{"doi":231},{"id":19,"text":234,"url":19,"identifiers":235},"10.1039\u002Ftf9605600648",{"doi":234},{"id":19,"text":237,"url":19,"identifiers":238},"Van Berkel R. W. M., 1982, Developments in Block Copolymers—I",{},{"id":19,"text":240,"url":19,"identifiers":241},"10.1002\u002Fapp.1979.070230412",{"doi":240},{"id":19,"text":243,"url":19,"identifiers":244},"10.1002\u002Fapp.1979.070230413",{"doi":243},false,{"id":247,"createTime":248,"updateTime":248,"relativeEntities":249,"slug":250,"properties":251,"entityType":48,"verifyStatus":49,"verifyTime":248,"verifyNote":50,"syncStatus":18,"languages":263,"translateLanguages":19,"viewCount":20,"primaryUrl":264,"fullTextUrl":19,"authors":265,"publicationType":128,"publisherRelationship":307,"citationCount":324,"citationInfo":325,"publishDate":327,"publishYear":328,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":329,"isForceReanalyzing":245},"1d7827a9-246c-471c-a8b8-14cb695c72a7","2024-10-05T22:44:06.732+00:00",[],"Superstructure-in-segmented-polyether-urethanes",{"mag":252,"keywords":254,"openalex":255,"abstract":257,"title":259,"doi":261},{"VOID":253},"2137137292",{},{"VOID":256},"W2137137292",{"EN":258},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The morphology of several series of segmented polyether–urethanes was studied. The “hard” segments contained urethane and urea linkages formed by 4,4′‐dicyclohexylmethane diisocyanate (Hylene W) and selected aliphatic and aromatic monomeric diamines (DA). The “soft” segments were composed of oligomeric poly(ethylene oxide) (PEO), poly(propylene oxide) (PPO), or both PEO and PPO. For studying the composition–morphology relationships, the molecular weight and relative content of PEO, and the relative content of PPO were varied systematically. Different diamines were used as chain extenders. The methods of wide‐angle x‐ray diffraction (WAXD), small‐angle x‐ray scattering (SAXS), polarizing microscopy, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) were employed in the investigation. The effects of PEO content on domain formation were very significant. Calculations based on a highly simplified model indicated that, for two adjacent molecules, if two hard segments are associated with each other, the probability for the association of the next two hard segments varies inversely with the third power of soft segment length. Copolymers composed of both POE and PPO displayed enhanced domain and anisotropic superstructure. The phenomenon was interpreted in terms of polymer incompatibility. The effects on morphology of different DA's as chain extenders were tentatively accounted for by the symmetry, hydrogen bonding, and rigidity of the hard segments as well as their incompatibility with the soft segments. The formation and deformation of superstructure were of particular interest. A model was proposed to account for the formation of the resultant anisotropic structure and mechanical properties.\u003C\u002Fjats:p>",{"EN":260},"Superstructure in segmented polyether–urethanes",{"VOID":262},"10.1002\u002Fpol.1975.180130302",[52],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fpol.1975.180130302",[266,288],{"id":267,"sortIndex":20,"researcher":19,"roles":268,"affiliations":269,"properties":281},"d95d6fa5-4350-4232-9f47-b1d32dcf76e6",[],[270],{"id":271,"sortIndex":20,"affiliation":272,"properties":19},"65a0a90c-9d59-4a20-a1a3-60436a1b7167",{"id":273,"createTime":274,"updateTime":275,"relativeEntities":276,"slug":277,"properties":278,"entityType":71,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"d578f260-e840-4580-952b-3b87a4f631f3","2024-08-31T19:00:24.102+00:00","2024-12-18T23:08:51.742+00:00",[],"Department-of-Chemistry-Princeton-University-Princeton-New-Jersey-08540",{"title":279},{"EN":280},"Department of Chemistry, Princeton University, Princeton New Jersey 08540",{"openalex":282,"orcid":284,"title":286},{"VOID":283},"A5034248263",{"VOID":285},"https:\u002F\u002Forcid.org\u002F0000-0003-0824-1266",{"EN":287},"Yaw‐Jen Chang",{"id":289,"sortIndex":112,"researcher":19,"roles":290,"affiliations":291,"properties":302},"07228039-3d5e-414c-b0c5-6d61a51d2751",[],[292],{"id":293,"sortIndex":20,"affiliation":294,"properties":19},"4f7a6037-60dc-4502-8e09-b33185b38895",{"id":295,"createTime":296,"updateTime":296,"relativeEntities":297,"slug":298,"properties":299,"entityType":71,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"56841fbd-1273-4e23-b128-37123f206751","2024-10-05T22:44:06.760+00:00",[],"Department-of-Chemical-Engineering-Polymer-Materials-Program-Princeton-University-Princeton-New-Jersey-08540",{"title":300},{"EN":301},"Department of Chemical Engineering Polymer Materials Program Princeton , University Princeton , New Jersey, 08540",{"openalex":303,"title":305},{"VOID":304},"A5020264597",{"EN":306},"Garth L. Wilkes",{"url":19,"publisher":308,"properties":317},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":309,"slug":10,"properties":310,"entityType":17,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20,"subjectFields":314,"manageAffiliations":315,"indexDatabases":316,"url":19,"thumbnailPath":19,"statistic":19,"gsStatistic":19,"type":19,"analyzePriority":19},[],{"issn":311,"eissn":312,"title":313},{"VOID":13},{"VOID":15},{"EN":10},[],[],[],{"volume":318,"pages":320,"issue":322},{"VOID":319},"13",{"VOID":321},"455-476",{"VOID":323},"3",82,{"total":324,"publishYear":19,"statisticByYear":326},{"2012":57,"2013":112,"2016":112,"2017":112,"2018":112,"2019":112,"2021":112},"1975-03-01",1975,[330,333,336,339,342,345,348,351,354,357,360,363,366,369,372,375,378,381,384,387,390,393,396,399,402,405],{"id":19,"text":331,"url":19,"identifiers":332},"10.1080\u002F15321797008068152",{"doi":331},{"id":19,"text":334,"url":19,"identifiers":335},"G. L.WilkesandS. L.Samuels Paper presented at the 19th Sagamore Army Materials Research Conference Sept. 1972;",{},{"id":19,"text":337,"url":19,"identifiers":338},"Burke J., 1973, Block and Graft Copolymers, 225",{},{"id":19,"text":340,"url":19,"identifiers":341},"10.1007\u002F978-1-4684-1842-2_7",{"doi":340},{"id":19,"text":343,"url":19,"identifiers":344},"10.1080\u002F00222346808212463",{"doi":343},{"id":19,"text":346,"url":19,"identifiers":347},"10.1007\u002FBF02160078",{"doi":346},{"id":19,"text":349,"url":19,"identifiers":350},"10.1080\u002F00222337308061138",{"doi":349},{"id":19,"text":352,"url":19,"identifiers":353},"S. L.CooperandR. W.Semour private communications.",{},{"id":19,"text":355,"url":19,"identifiers":356},"Chang Y. J., 1973, Polym. Prepr., 14, 1277",{},{"id":19,"text":358,"url":19,"identifiers":359},"10.1002\u002Fpol.1971.110091011",{"doi":358},{"id":19,"text":361,"url":19,"identifiers":362},"Samuels S. L., 1972, Polym. Prepr., 13, 999",{},{"id":19,"text":364,"url":19,"identifiers":365},"S. L.SamuelsandG. L.Wilkes J. Polym. Sci. Pt. A‐2 in press.",{},{"id":19,"text":367,"url":19,"identifiers":368},"10.1002\u002Fpolc.5070430115",{"doi":367},{"id":19,"text":370,"url":19,"identifiers":371},"10.1002\u002Fapp.1972.070160821",{"doi":370},{"id":19,"text":373,"url":19,"identifiers":374},"Kurata M., 1966, Polymer Handbook, IV‐38",{},{"id":19,"text":376,"url":19,"identifiers":377},"Pizzini L. C., 1967, Encyclopedia of Polymer Science and Technology, 120",{},{"id":19,"text":379,"url":19,"identifiers":380},"O'Malley J. J., 1968, Polym. Prepr., 10, 796",{},{"id":19,"text":382,"url":19,"identifiers":383},"Alexander I. E., 1969, X‐Ray Diffraction Methods in Polymer Science",{},{"id":19,"text":385,"url":19,"identifiers":386},"R. S.Stein private communication.",{},{"id":19,"text":388,"url":19,"identifiers":389},"Y. J.Chang Ph.D. thesis Dept. of Chemistry Princeton Univ. 1974.",{},{"id":19,"text":391,"url":19,"identifiers":392},"Hartshorne N. H., 1970, Crystals and the Polarizing Microscope",{},{"id":19,"text":394,"url":19,"identifiers":395},"Flory P. J., 1953, Principles of Polymer Chemistry",{},{"id":19,"text":397,"url":19,"identifiers":398},"Crowley J. D., 1966, J. Paint Technol., 38, 269",{},{"id":19,"text":400,"url":19,"identifiers":401},"10.1021\u002Fi360029a002",{"doi":400},{"id":19,"text":403,"url":19,"identifiers":404},"10.1002\u002Fjctb.5010030205",{"doi":403},{"id":19,"text":406,"url":19,"identifiers":407},"W. R.KrigbaumandJ. V.DawkinsinPolymer Handbook(cf. Ref. 14) pp.IV–331ff.",{},{"id":409,"createTime":410,"updateTime":411,"relativeEntities":412,"slug":413,"properties":414,"entityType":48,"verifyStatus":49,"verifyTime":410,"verifyNote":50,"syncStatus":18,"languages":428,"translateLanguages":19,"viewCount":20,"primaryUrl":429,"fullTextUrl":19,"authors":430,"publicationType":128,"publisherRelationship":465,"citationCount":482,"citationInfo":483,"publishDate":485,"publishYear":486,"citationAnalyzeStatus":487,"lastCitationAnalyze":488,"indexDatabases":19,"openAccess":19,"references":489,"isForceReanalyzing":245},"b65762c0-77e8-4cc3-80aa-51469b4c5801","2024-12-26T15:03:14.880+00:00","2026-01-15T22:22:46.769+00:00",[],"Melting-studies-of-poly-vinylidene-fluoride-and-its-blends-with-poly-methyl-methacrylate-",{"mag":415,"keywords":417,"openalex":418,"abstract":420,"title":422,"doi":424,"gsPaper":426},{"VOID":416},"2148710570",{},{"VOID":419},"W2148710570",{"EN":421},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Blends of poly(vinylidene fluoride) (PVF\u003Cjats:sub>2\u003C\u002Fjats:sub>) and poly(methyl methacrylate) exhibit complex melting behavior when crystallized at low undercoolings. Three crystals comprised of two different PVF\u003Cjats:sub>2\u003C\u002Fjats:sub> forms grow. Hoffman‐Weeks plots of the observed melting points \u003Cjats:italic>T\u003C\u002Fjats:italic>\u003Cjats:sub>\u003Cjats:italic>m\u003C\u002Fjats:italic>\u003C\u002Fjats:sub> of these crystals versus crystallization temperatures are constructed. The lowest‐melting‐point species, the α form, shows a change in slope which is attributed to fewer head‐to‐head PVF\u003Cjats:sub>2\u003C\u002Fjats:sub> units trapped in the crystal at higher temperatures. Defect energies in the crystal due to these units are calculated to be from 6.3 to 10.3 kJ\u002Fmol. Estimating lamellar thicknesses from the slopes of the two regions gives much more reasonable values when the high‐temperature data are used. Removal of kinetic effects that lower the observed \u003Cjats:italic>T\u003C\u002Fjats:italic>\u003Cjats:sub>\u003Cjats:italic>m\u003C\u002Fjats:italic>\u003C\u002Fjats:sub> by extrapolating the data to obtain \u003Cjats:italic>T\u003C\u002Fjats:italic>\u003Cjats:inline-graphic xmlns:xlink=\"http:\u002F\u002Fwww.w3.org\u002F1999\u002Fxlink\" xlink:href=\"graphic\u002Ftex2gif-stack-1.gif\" xlink:title=\"urn:x-wiley:00981273:media:POL180201207:tex2gif-stack-1\" \u002F> permits the thermodynamic interaction energy density \u003Cjats:italic>B\u003C\u002Fjats:italic> between the two polymers to be obtained. The low‐temperature α‐form data give \u003Cjats:italic>B\u003C\u002Fjats:italic> = −8.83 × 10\u003Cjats:sup>6\u003C\u002Fjats:sup> J\u002Fm\u003Cjats:sup>3\u003C\u002Fjats:sup>. The high‐temperature α‐form data and the \u003Cjats:italic>T\u003C\u002Fjats:italic>\u003Cjats:inline-graphic xmlns:xlink=\"http:\u002F\u002Fwww.w3.org\u002F1999\u002Fxlink\" xlink:href=\"graphic\u002Ftex2gif-stack-2.gif\" xlink:title=\"urn:x-wiley:00981273:media:POL180201207:tex2gif-stack-2\" \u002F> of the γ‐form crystals both show \u003Cjats:italic>B\u003C\u002Fjats:italic> to vary from −5.40 × 10\u003Cjats:sup>6\u003C\u002Fjats:sup> to −2.96 × 10\u003Cjats:sup>7\u003C\u002Fjats:sup> J\u002Fm\u003Cjats:sup>3\u003C\u002Fjats:sup> as the blend composition goes from 40.1 vol % to pure PVF\u003Cjats:sub>2\u003C\u002Fjats:sub>.\u003C\u002Fjats:p>",{"EN":423},"Melting studies of poly(vinylidene fluoride) and its blends with poly(methyl methacrylate)",{"VOID":425},"10.1002\u002Fpol.1982.180201207",{"VOID":427},"[]",[52],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fpol.1982.180201207",[431,450],{"id":432,"sortIndex":20,"researcher":19,"roles":433,"affiliations":434,"properties":445},"464a4c9c-91ad-435e-be4c-28d339292df4",[],[435],{"id":436,"sortIndex":20,"affiliation":437,"properties":19},"a08bd2ea-feba-4c94-b394-cf2b88ecc1b7",{"id":438,"createTime":439,"updateTime":439,"relativeEntities":440,"slug":441,"properties":442,"entityType":71,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"4c53c017-83e4-44f3-a598-d0fd63df863e","2024-12-26T15:03:14.895+00:00",[],"Polymer-Research-Institute-and-Materials-Research-Laboratory-University-of-Massachusetts-Amherst-Massachusetts-01003",{"title":443},{"EN":444},"Polymer Research Institute and Materials Research Laboratory, University of Massachusetts, Amherst, Massachusetts 01003",{"openalex":446,"title":448},{"VOID":447},"A5019335855",{"EN":449},"Bruce S. 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We have given particular attention to compositions containing low PEO concentrations. The crystallization behavior and the resultant microstructures of PEO are strongly perturbed by the presence of PMMA. 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The resulting enthalpy and entropy values indicated that while there is no interaction between adjacent amide groups in the polymer chain, there is, nevertheless, a substantial cooperative effect in the transverse hydrogen bond direction. We have also established that any analysis of hydrogen bond breaking in semicrystalline polymers (i.e., nylon 66) below the melting point should include a crystallinity correction factor. Extrapolation of our data above the melting point of nylon 66 yielded a 26% retention of hydrogen bonding.\u003C\u002Fjats:p>",{"EN":1338},"Hydrogen bonding in nylon 66 and model compounds",{"VOID":1340},"10.1002\u002Fpol.1985.180230310",[52],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fpol.1985.180230310",[1344,1361],{"id":1345,"sortIndex":112,"researcher":19,"roles":1346,"affiliations":1347,"properties":1358},"1f62a221-6c22-4087-9b05-7f68a36a1f8f",[],[1348],{"id":1349,"sortIndex":20,"affiliation":1350,"properties":19},"46d168a2-9c12-4fac-aec0-f8af13c733a8",{"id":1351,"createTime":1352,"updateTime":1352,"relativeEntities":1353,"slug":1354,"properties":1355,"entityType":71,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"58a567d3-c2f8-4c19-bdcf-314d800bb727","2024-09-21T20:56:16.030+00:00",[],"E-I-DuPont-de-Nemours-and-Company",{"title":1356},{"EN":1357},"E.I. 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M., 1978, Infrared and Raman Spectroscopy of Biological Molecules",{},{"id":19,"text":1472,"url":19,"identifiers":1473},"10.1016\u002F0009-2614(78)80319-4",{"doi":1472},{"id":19,"text":1475,"url":19,"identifiers":1476},"10.1093\u002Fcomjnl\u002F7.4.308",{"doi":1475},{"id":19,"text":1478,"url":19,"identifiers":1479},"10.1119\u002F1.1934101",{"doi":1478},{"id":19,"text":1481,"url":19,"identifiers":1482},"10.1366\u002F000370277774464156",{"doi":1481},{"id":19,"text":1484,"url":19,"identifiers":1485},"10.1063\u002F1.1694554",{"doi":1484},{"id":19,"text":1487,"url":19,"identifiers":1488},"10.1135\u002Fcccc19621749",{"doi":1487},{"id":19,"text":1490,"url":19,"identifiers":1491},"S.Mazur private communication 1982.",{},{"id":19,"text":1493,"url":19,"identifiers":1494},"Vinogradov S. 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A special form of Fick's law which accounts for the fact that penetrants in glassy polymers sorb into and diffuse through two different molecular environments provides the basis for the analysis of gas mixture permeation. 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